A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563361



Internal ID16004084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113398155..113400011hg38UCSC Ensembl
Innerchr13:114052470..114054326hg19UCSC Ensembl
Innerchr13:113100471..113102327hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381857
hg191857
hg181857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3447n54
Supporting Variantsnssv820635, nssv820638, nssv820648, nssv820636, nssv820650, nssv820651, nssv820643, nssv820646, nssv820633, nssv820640, nssv820649, nssv820642, nssv820647, nssv820645, nssv820634, nssv820641, nssv820630, nssv820644, nssv820631, nssv820632, nssv820637, nssv820639
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563361
Frequency
Sample Size17421
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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